Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGGAGGCGCGCACTGTGCGCGAG[C/G]CGCTGGGCCGCTACGAGGCGGCGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
SMTNL2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SMTNL2 - smoothelin like 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114974.1 | 113 | Missense Mutation | CCG,GCG | P,A 16 | NP_001108446.1 | |
NM_198501.2 | 113 | Intron | NP_940903.2 | |||
XM_005256622.3 | 113 | Missense Mutation | CCG,GCG | P,A 16 | XP_005256679.1 | |
XM_006721515.2 | 113 | Intron | XP_006721578.1 |